Clinical Trials Directory

Trials / Completed

CompletedNCT03057041

Intranasal Fentanyl for Pain Control During First-Trimester Uterine Aspiration

Intranasal Fentanyl for Pain Control During First-Trimester Uterine Aspiration: A Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
107 (actual)
Sponsor
University of Hawaii · Academic / Other
Sex
Female
Age
14 Years
Healthy volunteers
Accepted

Summary

Intranasal fentanyl has been found to be safe and effective in the reduction of pain among pediatric and adult populations. The investigators hypothesize that patients who receive 100 mcg of intranasal fentanyl for pain control before first-trimester uterine aspiration will report lower pain scores than those who receive placebo. The investigators will test this hypothesis using a randomized, double-blind, placebo-controlled trial comparing pain reported during uterine aspiration between patients who receive either intranasal fentanyl or intranasal saline prior to the procedure.

Conditions

Interventions

TypeNameDescription
DRUGFentanyl100 mcg of intranasal fentanyl, 50 mcg/ mL in each nostril via mucosal atomizer 15 minutes prior to procedure start
DRUGplacebo1 mL of sterile saline in each nostril via mucosal atomizer 15 minutes prior to procedure start

Timeline

Start date
2017-03-23
Primary completion
2018-05-30
Completion
2018-05-30
First posted
2017-02-17
Last updated
2018-06-13

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT03057041. Inclusion in this directory is not an endorsement.